ND6 - NADH dehydrogenase subunit 6-BMKCloudï½ç¾è¿å®¢äº

例如："NBL1", "4681", "drought"

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6775063 ND6

基因描述

Type	Description
Definition	NADH dehydrogenase subunit 6

研究结论

Date	Results	Publications
2021-04-03 13:30:00	Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency.	32162843
2019-11-23 12:46:00	Leber hereditary optic neuropathy caused by homoplasmic variant in ND6	30347014
2018-11-24 12:06:00	Mutations in the ND6, NDUFV1 or ACAD9 genes are responsible for the mitochondrial complex I deficiency.	29348607
2016-07-30 11:10:00	Compound mtDNA mutations of m.3635G > A and m.14502T > C presented with low penetration, and the patients with these compound mutations exhibited mild visual impairment.	24417559
2016-02-20 11:29:00	ND6 gene nonsense and missense mutations might promote cell migration and invasion in lung adenocarcinoma.	25934296

名称对应

Type	IDs
Gene	UniProtKB-ID: B4F446_HOMNE UniprotKB: B4F446 UniParc: UPI000005CE1B EMBL: KU131206, FM865409, MG025536, KX198084, FM865408, KC879692, KY751400, KJ533545, FM865410, KX198086, MK033602, MG025538, MG025540, KX198085, MG025539, KX198087, FM865407, KX198082, KX198088, MK123269, KJ533544, MK388903, AM948965, FM865411, MG025537
Nucleutide sequences	EMBL-CDS: CAR95812.1, CAQ37657.1, ANC95213.1, ASK06276.1, QEE94739.1, ANC95200.1, ANC95174.1, AUD37534.1, CAR95838.1, AGO20291.1, AUD37495.1, AUD37482.1, ANC95161.1, AHZ61470.1, ANC95135.1, AHZ61457.1, AMQ34022.1, CAR95864.1, AUD37508.1, QIT06505.1, CAR95851.1, QAU54317.1, ANC95187.1, AUD37521.1, CAR95825.1
Protein sequencees	RefSeq: YP_002124313.1
Others	UniRef100: UniRef100_B9EEZ1 UniRef90: UniRef90_P03923 UniRef50: UniRef50_P03923

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mRNA

Protein

UniprotKB

Description

Refseq

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全选

Pubmed编号	文献信息	发表日期	相关基因
32162843	Systematic analysis of a mitochondrial disease-causing ND6 mutation in mitochondrial deficiency. Mol Genet Genomic Med Deyu Chen , Qiongya Zhao , Jingting Xiong , Xiaoting Lou , Qinxia Han , Xiujuan Wei , Jie Xie , Xueyun Li , Huaibin Zhou , Lijun Shen , Yanling Yang , Hezhi Fang , Jianxin Lyu	2020-05-01	-
30347014	Progressive Bilateral Cecocentral Scotomata. JAMA Ophthalmol Maria Fernanda Abalem , Mark W Johnson , Thiran Jayasundera	2019-01-01	-
29348607	Evaluation of mitochondrial bioenergetics, dynamics, endoplasmic reticulum-mitochondria crosstalk, and reactive oxygen species in fibroblasts from patients with complex I deficiency. Sci Rep Guilhian Leipnitz , Al-Walid Mohsen , Anuradha Karunanidhi , Bianca Seminotti , Vera Y Roginskaya , Desiree M Markantone , Mateus Grings , Stephanie J Mihalik , Peter Wipf , Bennett Van Houten , Jerry Vockley	2018-01-18	-
24417559	Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635Gâ>âA and ND6 m.14502 Tâ>âC. Ophthalmic Genet. Xin Jin , Lifeng Wang , Yan Gong , Bing Chen , Yanhua Wang , Tingjun Chen , Shihui Wei	2015-01-01	-
25934296	Nonsense and missense mutation of mitochondrial ND6 gene promotes cell migration and invasion in human lung adenocarcinoma. BMC Cancer Yang Yuan , Weixing Wang , Huizhong Li , Yongwei Yu , Jin Tao , Shengdong Huang , Zhiyong Zeng	2015-01-01	ND6
24846978	[The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation]. Yi Chuan Xiangjuan Meng , Jinping Zhu , Min Gao , Sai Zhang , Fuxin Zhao , Juanjuan Zhang , Xiaoling Liu , Qiping Wei , Yi Tong , Minglian Zhang , Jia Qu , Minxin Guan	2014-04-01	ND6
24398099	Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy. Invest. Ophthalmol. Vis. Sci. Min Liang , Pingping Jiang , Feng Li , Juanjuan Zhang , Yanchun Ji , Yiqun He , Meifen Xu , Jinping Zhu , Xiangjuan Meng , Fuxin Zhao , Yi Tong , Xiaoling Liu , Yanhong Sun , Xiangtian Zhou , Jun Qin Mo , Jia Qu , Min-Xin Guan	2014-03-01	ND6
23813926	Severe infantile leigh syndrome associated with a rare mitochondrial ND6 mutation, m.14487T>C. Am J Med Genet A Mark Tarnopolsky , Brandon Meaney , Brian Robinson , Katherine Sheldon , Richard G Boles	2013-08-01	-
20801516	Simultaneous mutation detection in 90 retinal disease genes in multiple patients using a custom-designed 300-kb retinal resequencing chip. Ophthalmology Judith C Booij , Arne Bakker , Jamilia Kulumbetova , Youssef Moutaoukil , Bert Smeets , Joke Verheij , Hester Y Kroes , Caroline C W Klaver , Mary van Schooneveld , Arthur A B Bergen , Ralph J Florijn	2011-01-01	ND6, ND4, ND1, NR2E3, USH1C, OPTN, MERTK, PRPF8, TTC8, USH1G, CNGB1, CNGA1, CNGA3, BBS5, CRX, RDH12, EFEMP1, TRIM32, RIMS1, CRB1, AIPL1, ABCA4, PRPF31, BBS9, GNAT1, GRM6, GUCA1A, GUCY2D, CFH, APOA1, IMPDH1, ABCC6, CERKL, ARMS2, MITF, MYO7A, MYOC, NDP, NRL, OCA2, PAX3, PAX6, PDE6A, PDE6B, CNGB3, BBS7, CABP4, RPGRIP1, BBS1, BBS2, BBS4, OPN1LW, RDH5, PRPH2, RGR, RHO, RLBP1, NYX, ROM1, RP9, RP1, RP2, RPGR, OPN1SW, RPE65, RS1, CFB, SAG, CDH23, SEMA4A, PCDH15, ELOVL4, TIMP3, C2, TTPA, TULP1, USH2A, BEST1, CA4, CACNA1F, ALMS1, BBS10, CEP290, OPA3, MKKS, ADGRV1, ARL6, UNC119, PRPF3, LRAT
20599858	Screening the three LHON primary mutations in the general Chinese population by using an optimized multiplex allele-specific PCR. Clin. Chim. Acta Rui Bi , A-Mei Zhang , Dandan Yu , Diana Chen , Yong-Gang Yao	2010-11-11	ND6, ND4, ND1

研究热度

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